New substituted isocoumarins and Dihydroisocoumarins and their cytotoxic activities.
Veronika Hampl, Isolde Wetzel, Franz Bracher, Jürgen Krauss
Index: Sci. Pharm. 79(1) , 21-30, (2011)
Full Text: HTML
Abstract
New isocoumarins were prepared in an efficient way from 2-iodobenzoic acid derivatives and hept-1-yne in a Sonogashira reaction, followed by spontaneous cyclization. Catalytic hydrogenation gave the corresponding dihydroisocoumarins. A 4-chloroisocoumarin was prepared on an alternative pathway. Some of the new compounds showed moderate cytotoxic activities against a human leukemia cell line (HL 60).
Related Compounds
Related Articles:
1991-02-01
[J. Med. Chem. 34(2) , 491-6, (1991)]
Asymmetric allylic oxidation with biarylbisoxazoline-copper (I) catalysis. Andrus MB and Asgari D.
[Tetrahedron 56(32) , 5775-5780, (2000)]